FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term nephrotic syndrome type 8 ID (Ontology) DOID:0080389 (Human Disease)
Definition A familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25.
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 nephrotic syndrome type 8       1
 for disease ribbon | nephrotic syndrome type 8       1
 model of | nephrotic syndrome type 8       1
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monogenic disease
 |__familial nephrotic syndrome__
autosomal genetic disease        |
 |__autosomal recessive disease__|
nephrotic syndrome               |
 |__familial nephrotic syndrome__|
                                 nephrotic syndrome type 8  1 rec.
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Is a autosomal recessive disease
familial nephrotic syndrome
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MIM:615244